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Spirit Portable Liquid Oxygen

FDA UDI

Class II (US FDA UDI)

by Caire Inc.

Identity

Trade Name
Spirit Portable Liquid Oxygen FDA UDI
Generic Name
Portable liquid oxygen unit FDA UDI
Device Name
• Portable Liquid Oxygen Respiratory Equipment, Side Fill, 5 LPM, 20 PSI FDA UDI
Model / Reference
13103130 FDA UDI
Description
• Portable Liquid Oxygen Respiratory Equipment, Side Fill, 5 LPM, 20 PSI FDA UDI

Identifiers

Primary DI / UDI-DI
M766131031300 FDA UDI
510(k) Number
K080023 FDA UDI
FDA Product Code
BYJ FDA UDI
GMDN Term
Portable liquid oxygen unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5655 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Portable liquid oxygen unit

Spirit Portable Liquid Oxygen by Caire Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Portable liquid oxygen unit.

Cleared under the same submission

K080023 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Caire Inc.

Sources (1)

  • FDA UDI e0ef53c6-d74f-4c0e-abc4-db22391d2ebd 34 fields · synced May 30, 2026